BAMBUSA STANNUM PELLET [URIEL PHARMACY INC.]

  • Home
  • BAMBUSA STANNUM PELLET [URIEL PHARMACY INC.]

BAMBUSA STANNUM PELLET [URIEL PHARMACY INC.]
PDF | XML
NDC 48951-2019-2
Set ID e57ff1b4-b8ca-48bd-a7ae-2596b1bbe27a
Category HUMAN OTC DRUG LABEL
Packager Uriel Pharmacy Inc.
Generic Name
Product Class
Product Number
Application Number
View All Sections
  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

  • DOSAGE & ADMINISTRATION

    Dissolve pellets under the tongue 3-4
    times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.

  • ACTIVE INGREDIENT

    Active Ingredients: Bambusa (Bamboo) 6X, Betonica (Wood betony) 6X, Disci intervertebrales (Bovine intervertebral discs of the cervical, thoracic and lumbar spine) 6X, Rosmarinus (Rosemary) 6X, Formica (Red wood ant) 7X, Stannum met. (Metallic tin) 7X, Jasper (Semiprecious stone) 12X, Equisetum (Common horsetail) 15X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Sucrose, Lactose

  • PURPOSE

    Use: Temporary relief of headache.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

  • QUESTIONS

    Questions? Call 866.642.2858
    Uriel, East Troy WI 53120
    www.urielpharmacy.com

  • PRINCIPAL DISPLAY PANEL

    BambusaStannumPellets

  • INGREDIENTS AND APPEARANCE
    BAMBUSA STANNUM 
    bambusa stannum pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-2019
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BAMBUSA VULGARIS WHOLE (UNII: WCD45M1BSK) (BAMBUSA VULGARIS WHOLE - UNII:WCD45M1BSK) BAMBUSA VULGARIS WHOLE6 [hp_X]
    STACHYS OFFICINALIS (UNII: UO9989Y17N) (STACHYS OFFICINALIS - UNII:UO9989Y17N) STACHYS OFFICINALIS6 [hp_X]
    ROSMARINUS OFFICINALIS FLOWERING TOP (UNII: 8JM482TI79) (ROSMARINUS OFFICINALIS FLOWERING TOP - UNII:8JM482TI79) ROSMARINUS OFFICINALIS FLOWERING TOP6 [hp_X]
    BOS TAURUS INTERVERTEBRAL DISC (UNII: 0A04Z76C13) (BOS TAURUS INTERVERTEBRAL DISC - UNII:0A04Z76C13) BOS TAURUS INTERVERTEBRAL DISC6 [hp_X]
    FORMICA RUFA (UNII: 55H0W83JO5) (FORMICA RUFA - UNII:55H0W83JO5) FORMICA RUFA7 [hp_X]
    TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5) TIN7 [hp_X]
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE12 [hp_X]
    EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (EQUISETUM ARVENSE TOP - UNII:1DP6Y6B65Z) EQUISETUM ARVENSE TOP15 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    LACTOSE (UNII: J2B2A4N98G)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize3mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-2019-21350 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product09/01/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/01/2009
    Labeler - Uriel Pharmacy Inc. (043471163)
    Establishment
    NameAddressID/FEIBusiness Operations
    Uriel Pharmacy Inc.043471163manufacture(48951-2019)
View All Sections

Related Drugs

Search DailyMed Drugs